Use of eugenol polyethers and eugenol polyether siloxanes as wetting agents
a technology which is applied in the field of use of eugenol polyether and eugenol polyether siloxanes as wetting agents, and can solve the problems of significant lowering of static surface tension, significant foaming, and large restriction of fluorinated surfactants us
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Benefits of technology
Problems solved by technology
Method used
Examples
example 1
of a Eugenol-Based Polyether (Inventive)
[0281]A 5 liter autoclave was initially charged with 351 g of eugenol, and 100 ppm (based on the overall mixture) of a zinc hexacyanocobaltate double metal cyanide catalyst was added. The reactor was inertized by injecting nitrogen to 3 bar and subsequent decompression to standard pressure. This operation was repeated twice more. While stirring, the contents of the reactor were heated to 100° C. and evacuated to about 20 mbar to remove volatile components. After 30 min, the temperature was increased to 130° C. and 100 g of propylene oxide were metered into the evacuated reactor to activate the catalyst. The internal pressure at first rose to about 0.8 bar. The pressure began to drop slowly and had dropped to −0.1 bar after about 7 minutes. A further 50 g of PO were then metered in, and then the pressure rose to 0.8 bar once more. After 12 minutes, the pressure had dropped to −0.1 bar and a further 50 g of PO were metered in. Once the pressure ...
example 2
of a Eugenol-Based Polyether (Inventive)
[0282]A 5 liter autoclave was initially charged with 164.2 g of eugenol, and 100 ppm (based on the overall mixture) of a zinc hexacyanocobaltate double metal cyanide catalyst was added. The reactor was inertized by injecting nitrogen to 3 bar and subsequent decompression to standard pressure. This operation was repeated twice more. While stirring, the contents of the reactor were heated to 100° C. and evacuated to about 20 mbar to remove volatile components. After 30 min, the temperature was increased to 130° C. and 70 g of propylene oxide were metered into the evacuated reactor to activate the catalyst. The internal pressure at first rose to about 0.8 bar. The pressure began to drop slowly and had dropped to −0.4 bar after about 30 minutes. Slow, continuous addition of propylene oxide was then commenced. After addition of a further 56 g of PO the pressure rose to 0.7 bar and then dropped suddenly to −0.8 bar after addition of a total of 200 g...
example 3
of a Eugenol-Based Polyether (Inventive)
[0283]A 5 liter autoclave was initially charged with 544 g of eugenol, and 200 ppm (based on the overall mixture) of a zinc hexacyanocobaltate double metal cyanide catalyst was added. The reactor was inertized by injecting nitrogen to 3 bar and subsequent decompression to standard pressure. This operation was repeated twice more. While stirring, the contents of the reactor were heated to 80° C. and evacuated to about 20 mbar to remove volatile components. After 30 min, the temperature was increased to 140° C. and 80 g of propylene oxide were metered into the evacuated reactor to activate the catalyst. The internal pressure at first rose to about 0.6 bar. The pressure began to drop slowly and had dropped to −0.2 bar after about 10 minutes. A further 74 g of PO were then metered in which caused the pressure to drop slowly to −0.8 bar over 60 minutes. Metered addition of a mixture of 612 g of ethylene oxide and 691 g of propylene oxide was then c...
PUM
Property | Measurement | Unit |
---|---|---|
temperatures | aaaaa | aaaaa |
particle sizes | aaaaa | aaaaa |
flow rate | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com